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Sign in to claim this brandAi Nile Inc
US
Last updated May 25, 2026
What Ai Nile Inc makes
Ai Nile Inc develops mobile applications designed to assist users in managing medication schedules through automated reminders and notifications. These software-based solutions are intended for personal use, helping individuals adhere to prescribed treatment plans via push alerts and tracking features.
The company’s products fall under FDA’s Class I regulatory category and are listed in the FDA’s Unique Device Identifier (UDI) database. Ai Nile Inc operates from the United States, where its software-based devices are authorised for commercial distribution.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Ai Nile Inc manufacture?
Ai Nile Inc specializes in medication reminder application software, which helps users manage prescribed treatment plans through automated alerts and tracking features. These are software-based solutions designed for personal use on mobile devices, ensuring patients stay on schedule with their medication routines.
Where is Ai Nile Inc based, and does that affect its regulatory status?
Ai Nile Inc is based in the United States, where its software-based devices are authorised for commercial distribution. The company’s location aligns with FDA regulatory oversight, as its products fall under the FDA’s jurisdiction for software-as-a-medical-device (SaMD) classification.
Which regulatory registries list Ai Nile Inc’s devices?
Ai Nile Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which is a centralised registry for tracking medical devices authorised in the US. This inclusion ensures transparency and traceability for regulatory and market surveillance purposes.
How are Ai Nile Inc’s devices classified under FDA regulations?
Ai Nile Inc’s medication reminder applications are classified as FDA Class I devices. This classification is typically assigned to low-risk products, including software that poses minimal risk to patients when used as intended—such as automated reminders for medication adherence—without active patient monitoring or complex interventions.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 118148877
Catalogue (3)
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